Variant report

Variant	rs9359503
Chromosome Location	chr6:82530332-82530333
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:82476333..82478960-chr6:82529549..82531643,2	MCF-7	breast:

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1000276	0.90[CHB][hapmap];0.82[JPT][hapmap]
rs12524158	0.83[CHB][hapmap]
rs1931623	1.00[CEU][hapmap];0.89[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs194615	0.83[CHB][hapmap]
rs1981090	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.92[TSI][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35948269	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6924759	0.83[CHB][hapmap]
rs6931358	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6941969	0.83[CHB][hapmap]
rs733413	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9359505	0.89[CEU][hapmap];0.84[CHB][hapmap]
rs9361861	1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap];0.93[YRI][hapmap];0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830712	chr6:82491029-82654531	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82517200-82530600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr6:82522800-82531400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr6:82523800-82532600	Enhancers	Stomach Mucosa	stomach
4	chr6:82528000-82532000	Enhancers	Primary B cells from cord blood	blood
5	chr6:82528000-82532400	Enhancers	Primary B cells from peripheral blood	blood
6	chr6:82528600-82530800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:82529000-82530600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr6:82529000-82530600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr6:82529000-82530800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr6:82529000-82532600	Enhancers	HepG2	liver
11	chr6:82529400-82530600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:82529400-82544000	Weak transcription	Right Atrium	heart
13	chr6:82529600-82530600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:82529600-82532200	Weak transcription	Gastric	stomach
15	chr6:82530000-82530600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:82530000-82530800	Enhancers	Fetal Intestine Small	intestine
17	chr6:82530200-82530400	Flanking Active TSS	Colonic Mucosa	Colon
18	chr6:82530200-82530400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
19	chr6:82530200-82530600	Flanking Active TSS	Duodenum Mucosa	Duodenum
20	chr6:82530200-82530600	Enhancers	Fetal Lung	lung
21	chr6:82530200-82530600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr6:82530200-82530800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr6:82530200-82531000	Flanking Active TSS	Liver	Liver
24	chr6:82530200-82531200	Enhancers	Fetal Intestine Large	intestine
25	chr6:82530200-82531200	Enhancers	Ovary	ovary
26	chr6:82530200-82531200	Enhancers	Small Intestine	intestine

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